# A unified classification system for HIV-1 5’ long terminal repeats

**Authors:** Xing Guo, Dan Yu, Mengying Liu, Hanping Li, Mingyue Chen, Xinyu Wang, Xiuli Zhai, Bohan Zhang, Yanglan Wang, Caiqing Yang, Chunlei Wang, Yongjian Liu, Jingwan Han, Xiaolin Wang, Jingyun Li, Lei Jia, Lin Li

PMC · DOI: 10.1371/journal.pone.0301809 · 2024-05-02

## TL;DR

This study creates a unified classification system for HIV-1 5’ LTRs, improving understanding of viral origin, spread, and therapy.

## Contribution

A systematic and phylogenetic classification system for HIV-1 5’ LTRs is proposed for the first time.

## Key findings

- 83 representatives and 14 consensus sequences were identified for 2 groups, 6 subtypes, 6 sub-subtypes, and 9 CRFs.
- 16 out of 22 clinical isolates showed consistent subtype classification with previous systems.
- 6 strains with recombination events showed different classifications, affecting transcription factor binding sites.

## Abstract

The HIV-1 provirus mainly consists of internal coding region flanked by 1 long terminal repeats (LTRs) at each terminus. The LTRs play important roles in HIV-1 reverse transcription, integration, and transcription. However, despite of the significant study advances of the internal coding regions of HIV-1 by using definite reference classification, there are no systematic and phylogenetic classifications for HIV-1 5’ LTRs, which hinders our elaboration on 5’ LTR and a better understanding of the viral origin, spread and therapy. Here, by analyzing all available resources of 5’ LTR sequences in public databases following 4 recognized principles for the reference classification, 83 representatives and 14 consensus sequences were identified as representatives of 2 groups, 6 subtypes, 6 sub-subtypes, and 9 CRFs. To test the reliability of the supplemented classification system, the constructed references were applied to identify the 5’ LTR assignment of the 22 clinical isolates in China. The results revealed that 16 out of 22 tested strains showed a consistent subtype classification with the previous LTR-independent classification system. However, 6 strains, for which recombination events within 5’ LTR were demonstrated, unexpectedly showed a different subtype classification, leading a significant change of binding sites for important transcription factors including SP1, p53, and NF-κB. The binding change of these transcriptional factors would probably affect the transcriptional activity of 5’ LTR. This study supplemented a unified classification system for HIV-1 5’ LTRs, which will facilitate HIV-1 characterization and be helpful for both basic and clinical research fields.

## Linked entities

- **Proteins:** SP1 (Sp1 transcription factor), TP53 (tumor protein p53), NFKB1 (nuclear factor kappa B subunit 1)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, SP1 (Sp1 transcription factor) [NCBI Gene 6667]
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11065288/full.md

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Source: https://tomesphere.com/paper/PMC11065288